cas 1705578-22-8|| where to buy potassium (3-((2-bromophenyl)amino)-3-oxopropyl)trifluoroborate

Nom du produit:potassium (3-((2-bromophenyl)amino)-3-oxopropyl)trifluoroborate

IUPAC Name:potassium {2-[(2-bromophenyl)carbamoyl]ethyl}trifluoroboranuide

: CAS：1705578-22-8; Formule moléculaire：C9H9BBrF3KNO; Pureté：95%

Unité d'emballage	Stock disponible	Prix($)
CM211556-250mg	in stock	ľǪǪ
CM211556-1g	in stock	ƥĲȃ
CM211556-5g	in stock	ƈȃǪǪ

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: N° CAS:1705578-22-8; Formule moléculaire:C9H9BBrF3KNO; Point de fusion:-; Code SMILES:F[B-](F)(CCC(NC1=CC=CC=C1Br)=O)F.[K+]; Densité:

: Numéro de catalogue:CM211556; Poids moléculaire:333.98; Point d'ébullition:; N° Mdl:; Stockage:Store at 2-8°C.

: Borates; Borates are classified as critical materials, they are the main source of boron and have a variety of industrial applications. Organic trifluoroborate is stable to heat, air and humidity, and is a very convenient crystalline boric acid compound. Since it has a tetra-coordinated boronic acid structure after the substitution of fluorine, it does not exhibit Lewis acidity and is stable to oxidation conditions. In addition, it can be regarded as the protector of boronic acid and boronic acid ester, which can be converted into each other. The compound can generally exist stably in organic solvents, but will decompose in protic solvents to liberate trivalent boron, so it can be directly used as a substrate for Suzuki coupling. The difference between trifluoroborate and boric acid is that it must exist in a monomeric form, so the equivalent weight can be closely controlled.